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内皮素-1基因多态性与类风湿关节炎患者的高血压相关。

Polymorphisms of the endothelin-1 gene associate with hypertension in patients with rheumatoid arthritis.

作者信息

Panoulas Vasileios F, Douglas Karen M J, Smith Jacqueline P, Taffé Patrick, Stavropoulos-Kalinoglou Antonios, Toms Tracey E, Elisaf Moses S, Nightingale Peter, Kitas George D

机构信息

Department of Rheumatology, Dudley Group of Hospitals NHS Trust, Russells Hall Hospital, Dudley, West Midlands, UK.

出版信息

Endothelium. 2008 Jul-Aug;15(4):203-12. doi: 10.1080/10623320802228708.

Abstract

Rheumatoid arthritis (RA) associates with excess cardiovascular (CV) morbidity and mortality. Hypertension, a highly prevalent entity in RA, has been associated with the endothelin-1 (ET-1) gene locus (EDN1) in some groups, such as Afro-Caribbean, the obese, and in low-renin states, but not in the general population as a whole. High levels of plasma ET-1 have been observed in RA. This study evaluated the potential association of EDN1 gene locus and serum ET-1 levels with hypertension in patients with RA. Genomic DNA and serum samples were collected from 397 well-characterized RA patients; DNA was also available from 401 local general population controls without RA. To explore the overall relevance of EDN1, two suitable single-nucleotide polymorphisms (SNPs), rs1800541 and rs5370, were selected and haplotype analysis was performed. Both SNPs were identified using real-time polymerase chain reaction (PCR) and melting curve analysis. Genetic analysis was related to hypertension as dichotomous trait and to blood pressure indices as continuous variables. Serum endothelin levels were also assessed in the RA patients. No genotype or haplotype differences were observed between RA and control subjects. Within RA, logistic regression analysis of each SNP separately revealed a threefold increase in the adjusted odds of being hypertensive of rs5370 TT homozygotes compared to GG homozygotes (OR = 2.89, 95%CI: 1.02 to 8.19). After adjustment for multiple potential confounders, haplotype analysis revealed an additive effect of the rs1800541-rs5370 T-T haplotype on hypertension (OR = 2.96, 95%CI: 1.28 to 6.86; p = .011), systolic blood pressure (SBP) (beta = 6.75 +/- 2.57 mm Hg; p = .009), and pulse pressure (PP) (beta = 4.37 +/- 2.12 mm Hg; p = .040). There was an increased prevalence of raised ET-1 levels amongst hypertensive RA patients, whereas a similar trend was observed for T-T haplotype carriers. RA patients who carry the rs1800541-rs5370 T-T EDN1 haplotype appear more likely to be hypertensive with an increased SBP and PP. These findings, if replicated in future studies, could be used as a screening tool for RA patients at increased hypertension, and thus cardiovascular, risk.

摘要

类风湿关节炎(RA)与心血管(CV)疾病的高发病率和高死亡率相关。高血压在RA患者中非常普遍,在一些人群中,如非洲加勒比裔、肥胖人群以及低肾素状态患者中,高血压与内皮素-1(ET-1)基因位点(EDN1)有关,但在总体人群中并非如此。在RA患者中观察到血浆ET-1水平升高。本研究评估了EDN1基因位点和血清ET-1水平与RA患者高血压之间的潜在关联。收集了397例特征明确的RA患者的基因组DNA和血清样本;同时也收集了401例无RA的当地普通人群对照的DNA样本。为了探究EDN1的整体相关性,选择了两个合适的单核苷酸多态性(SNP),即rs1800541和rs5370,并进行了单倍型分析。通过实时聚合酶链反应(PCR)和熔解曲线分析鉴定这两个SNP。遗传分析将高血压作为二分性状,将血压指标作为连续变量。还评估了RA患者的血清内皮素水平。在RA患者和对照受试者之间未观察到基因型或单倍型差异。在RA患者中,对每个SNP分别进行逻辑回归分析显示,与GG纯合子相比,rs5370 TT纯合子患高血压的校正比值增加了两倍(OR = 2.89,95%CI:1.02至8.19)。在对多个潜在混杂因素进行校正后,单倍型分析显示rs1800541 - rs5370 T - T单倍型对高血压(OR = 2.96,95%CI:1.28至6.86;p = 0.011)、收缩压(SBP)(β = 6.75±2.57 mmHg;p = 0.009)和脉压(PP)(β = 4.37±2.12 mmHg;p = 0.040)有累加效应。高血压RA患者中ET-1水平升高的患病率增加,而T - T单倍型携带者也观察到类似趋势。携带rs1800541 - rs5370 T - T EDN1单倍型的RA患者似乎更易患高血压,且SBP和PP升高。如果这些发现能在未来研究中得到重复验证,可作为RA患者高血压及心血管疾病风险增加的筛查工具。

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